Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K014209 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICA... | 1 | 12/04/2014 |
FEI # 3001451571 ConMed Corporation |
| ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MED... | 1 | 12/04/2014 |
FEI # 3001451571 ConMed Corporation |
| ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO PHILIPS MEDI... | 1 | 12/04/2014 |
FEI # 3001451571 ConMed Corporation |
| PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. The PadPro(R... | 2 | 05/13/2013 |
FEI # 3001451571 ConMed Corporation |
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